Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
147251 BAA10g31660 A10 23025671 C T synonymous_variant LOW c.1014G>A|p.Lys338Lys S275
147252 BAA10g31660 A10 23026179 G A missense_variant MODERATE c.506C>T|p.Pro169Leu S35
147253 BAA10g31660 A10 23027446 G A synonymous_variant LOW c.111C>T|p.Ile37Ile S172
S217
147254 BAA10g31650 A10 23027682 G A upstream_gene_variant MODIFIER c.-2983C>T| S138
147255 BAA10g31670 A10 23028159 C T missense_variant MODERATE c.386G>A|p.Arg129Lys S2
147256 BAA10g31670 A10 23028220 C T missense_variant MODERATE c.325G>A|p.Ala109Thr S200
147257 BAA10g31670 A10 23028371 C T synonymous_variant LOW c.174G>A|p.Lys58Lys S169
147258 BAA10g31670 A10 23028516 G A missense_variant MODERATE c.29C>T|p.Thr10Ile S71
147259 BAA10g31680 A10 23028761 C T synonymous_variant LOW c.594G>A|p.Lys198Lys S281
147260 BAA10g31650 A10 23029592 C T upstream_gene_variant MODIFIER c.-4893G>A| S188
147261 BAA10g31660 A10 23031328 C T upstream_gene_variant MODIFIER c.-3772G>A| S177
147262 BAA10g31690 A10 23032846 G A missense_variant MODERATE c.241C>T|p.Leu81Phe S284
147263 BAA10g31690 A10 23033053 G A missense_variant MODERATE c.34C>T|p.Leu12Phe S231
147264 BAA10g31680 A10 23034505 G A upstream_gene_variant MODIFIER c.-3981C>T| S191
147265 BAA10g31700 A10 23039865 G A intron_variant MODIFIER c.2098-410C>T| S205
147266 BAA10g31700 A10 23039944 G A intron_variant MODIFIER c.2098-489C>T| S241
147267 BAA10g31700 A10 23043463 G A stop_gained HIGH c.2014C>T|p.Gln672* S35
147268 BAA10g31700 A10 23043836 G A missense_variant MODERATE c.1717C>T|p.Pro573Ser S174
147269 BAA10g31700 A10 23043890 C T missense_variant MODERATE c.1663G>A|p.Glu555Lys S146
147270 BAA10g31700 A10 23043947 C T missense_variant MODERATE c.1606G>A|p.Ala536Thr S302
147271 BAA10g31710 A10 23044280 G A upstream_gene_variant MODIFIER c.-3014G>A| S158
147272 BAA10g31700 A10 23044311 C T splice_region_variant&intron_variant LOW c.1596+5G>A| S236
147273 BAA10g31700 A10 23044747 G A missense_variant MODERATE c.1165C>T|p.Pro389Ser S216
147274 BAA10g31700 A10 23044969 C T missense_variant MODERATE c.943G>A|p.Val315Ile S12
147275 BAA10g31700 A10 23045074 C T missense_variant MODERATE c.838G>A|p.Asp280Asn S169